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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924218Generated: November 2, 2026

6-Amino-3-chloropyridazine → 6-Chloro-3-methyl-2-(trifluoromethyl)imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/1924218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Amino-3-chloropyridazineHCID 21643—
Reactant3-Bromo-1,1,1-trifluorobutan-2-oneHCID 2736410—
Solvent1,2-DimethoxyethaneHCID 8071—
Product6-Chloro-3-methyl-2-(trifluoromethyl)imidazo[1,2-b]pyridazineHCID 53629153—

Reaction Steps

A solution of 6-chloro-3-aminopyridazine x34 (3.16 g, 1 eq, 24.2 mmol) and 3-bromo-1,1,1-trifluorobutan-2-one (5 g, 1 eq, 24.4 mmol) in 1,2-dimethoxyethane (100 ml) is refluxed during 17 hours. After cooling to room temperature and filtration, the solvent is removed under reduced pressure and the crude mixture is purified by preparative chromatography on silicagel (CH2Cl2/MeOH/NH4OH: 98/2/0.2 (v/v/v)) leading to 6-chloro-3-methyl-2-(trifluoromethyl)imidazo[1,2-b]pyridazine x35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178533B2
Source datasetuspto-grants-2012_05
ORD IDord-2ff9af8d76a245e9917826b3c9361a5d
Source noteuspto-grants-2012_05